Vacuum Distillation of Aluminum and Silicon via Carbothermal Reduction of Their Oxides with Concentrated Solar Energy

- Organization:
- The Minerals, Metals and Materials Society
- Pages:
- 5
- File Size:
- 182 KB
- Publication Date:
- Jan 1, 2011
Abstract
"Using concentrated solar radiation as the energy source of high-temperature process heat, the carbothermal reductions of Al2O3 to Al and SiO2 to Si were examined thermodynamically and demonstrated experimentally at vacuum pressures. Reducing the system pressure favors Al(g) and Si(g) formation, enabling their vacuum distillation and avoiding contamination by carbides and/or oxycarbides. Exploratory experimentation in a solar reactor was performed with mixtures of charcoal with alumina and silica in the ranges of 1300-2000 K and 1997–2263 K, respectively, at 10-3 bar by direct exposure to concentrated thermal radiation. Distilled samples contained up to 19 wt% of Al in Al-Al2O3 mixtures and 79 wt% of Si in Si-SiO2 mixtures. When the reducing agent is derived from a biomass source, the solar-driven carbothermal processes are CO2 neutral.IntroductionMetallurgical extractive processes for producing Al1-2 from Al2O3 and Si3-6 from SiO2 are characterized by their high specific energy consumption and concomitant emissions. Alternatively, concentrated solar energy can be used as a high-temperature heat source to drive the carbothermal reductions and, thus, avoid greenhouse gas emissions and other pollutants derived from fossil-fuel-based processes7-12. When the reducing agent is biomass charcoal, the solar-driven carbothermal reduction is CO2 neutral. The carbothermal reductions of Al2O3 and SiO2 are represented by the simplified overall stoichiometric reactions:"
Citation
APA:
(2011) Vacuum Distillation of Aluminum and Silicon via Carbothermal Reduction of Their Oxides with Concentrated Solar EnergyMLA: Vacuum Distillation of Aluminum and Silicon via Carbothermal Reduction of Their Oxides with Concentrated Solar Energy. The Minerals, Metals and Materials Society, 2011.